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Baby Bharathi Needs Your Support To Fight SMA

Jagadeesh and Ezhilarasi's 1 year, 9 months old daughter, Bharathi, has been diagnosed with Spinal Muscular Atrophy (SMA) type 2- a rare disease that affects almost 1 in 10,000 babies worldwide. This disease progresses rapidly and in most cases kills the child before they turn 2 years old. Unfortunately, there is no treatment for SMA in India. Bharathi needs Zolgensma, a one-time gene replacement therapy, and it needs to be imported. Called the world's costliest drug, it costs 16 crore rupees and is more expensive than any family can afford alone. The only way her parents can put together such a huge amount is with your help. She needs your love and support you can help her too. Please donate whatever you can! #SMA #CureSMA #spinalmascularatrophyPlease share, support & contribute as much as possible. Nothing is small or big. Every penny counts. Thank you all in advance...

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